Variant #0000517899 (NC_000003.11:g.130720063G>T, NC_000003.11(NM_001001486.1):c.2630-1G>T (ATP2C1))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.130720063G>T
DNA change (hg38) g.131001219G>T
Published as ATP2C1(NM_001199179.3):c.2630-1G>T
ISCN -
DB-ID ASTE1_000003
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP2C1 NM_001001486.1 +/. - c.2630-1G>T r.spl? p.?
ASTE1 NM_014065.2 +/. - c.*12838C>A r.(=) p.(=)


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